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Showing results (161-170 of 282) with videos related to

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Hepatology (Baltimore, Md.)|December 26, 2006
Linkage between a new splicing site mutation in the MDR3 alias ABCB4 gene and intrahepatic cholestasis of pregnancyGudrun Schneider, Teresa C Paus, Gerd A Kullak-Ublick, et al.
Journal of the American Society of Nephrology : JASN|December 26, 2001
Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 geneHeymut Omran, GÜrsel Sasmaz, Karsten Häffner, et al.
Plos One|April 26, 2019
VarWatch-A stand-alone software tool for variant matchingBroder Fredrich, Marcus Schmöhl, Olaf Junge, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|December 14, 2007
Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantationM Mezger, M Steffens, C Semmler, et al.
Experimental Dermatology|August 22, 2003
Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective lociP Hensen, C Windemuth, U Hüffmeier, et al.
Human Genetics|February 8, 2006
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosisFrauke Stanke, Tim Becker, Harry Cuppens, et al.
Human Mutation|August 19, 2006
KCNQ4: a gene for age-related hearing impairment?E Van Eyken, L Van Laer, E Fransen, et al.
Human Molecular Genetics|February 28, 2009
A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylationOsman El-Maarri, Michael S Kareta, Thomas Mikeska, et al.
Kidney International|June 2, 1998
Beta-2 adrenoceptor genetic variation is associated with genetic predisposition to essential hypertension: The Bergen Blood Pressure StudyB Timmermann, R Mo, F C Luft, et al.
Blood|October 25, 2007
Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 expression in monocyte-derived dendritic cellsMarkus Mezger, Michael Steffens, Melanie Beyer, et al.
Pageof 29

Showing results (161-170 of 282) with videos related to

Sort By:
Pageof 29
Hepatology (Baltimore, Md.)|December 26, 2006
Linkage between a new splicing site mutation in the MDR3 alias ABCB4 gene and intrahepatic cholestasis of pregnancyGudrun Schneider, Teresa C Paus, Gerd A Kullak-Ublick, et al.
Journal of the American Society of Nephrology : JASN|December 26, 2001
Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 geneHeymut Omran, GÜrsel Sasmaz, Karsten Häffner, et al.
Plos One|April 26, 2019
VarWatch-A stand-alone software tool for variant matchingBroder Fredrich, Marcus Schmöhl, Olaf Junge, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|December 14, 2007
Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantationM Mezger, M Steffens, C Semmler, et al.
Experimental Dermatology|August 22, 2003
Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective lociP Hensen, C Windemuth, U Hüffmeier, et al.
Human Genetics|February 8, 2006
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosisFrauke Stanke, Tim Becker, Harry Cuppens, et al.
Human Mutation|August 19, 2006
KCNQ4: a gene for age-related hearing impairment?E Van Eyken, L Van Laer, E Fransen, et al.
Human Molecular Genetics|February 28, 2009
A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylationOsman El-Maarri, Michael S Kareta, Thomas Mikeska, et al.
Kidney International|June 2, 1998
Beta-2 adrenoceptor genetic variation is associated with genetic predisposition to essential hypertension: The Bergen Blood Pressure StudyB Timmermann, R Mo, F C Luft, et al.
Blood|October 25, 2007
Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 expression in monocyte-derived dendritic cellsMarkus Mezger, Michael Steffens, Melanie Beyer, et al.
Pageof 29